Silver–Russell syndrome, also called Silver–Russell dwarfism, is a rare congenital growth disorder. In the United States it is usually referred to as Russell–Silver syndrome, and Silver–Russell syndrome elsewhere. It is one of 200 types of dwarfism and one of five types of primordial dwarfism.
Silver–Russell syndrome occurs in approximately one out of every 50,000 to 100,000 births. Males and females seem to be affected with equal frequency.[1]
Signs and symptoms
Although confirmation of a specific genetic marker is in a significant number of individuals, there are no tests to clearly determine if this is what a person has. As a syndrome, a diagnosis is typically given for children upon confirmation of the presence of several symptoms listed below.[2]
The average adult height for patients without growth hormone treatment is 4'11" (149.9 cm) for males and 4'7" (139.7 cm) for females.[3]
Cause
Its exact cause is unknown, but present research points toward a genetic and epigenetic component, possibly following maternal genes on chromosomes 7 and 11.[4] Half of patients with Silver–Russell syndrome do not have an identified molecular etiology which suggests the involvement of other unknown genes. [5] Chromosomal imbalances of HMGA2 (high mobility AT-hook 2) located on chromosome 12 chromosome have been implicated with patients who do not have a classically identified genetic cause.[5]
It is estimated that approximately 50% of Silver–Russell patients have hypomethylation of H19 and IGF2.[6] This is thought to lead to low expression of IGF2 and over-expression of the H19 gene.[7]
In 10% of the cases, the syndrome is associated with maternal uniparental disomy (UPD) on chromosome 7.[4] This is the result of non-disjunction, where the person receives two copies of chromosome 7 from the mother (maternally inherited) rather than one from each parent. Normal expression requires IGF2 genes to be received from both parents, this may result in the same condition found in those with normal chromosomal inheritance but duplication events or hypomethylation.[8]
Other genetic causes such as duplications, deletions and chromosomal aberrations have also linked to Silver–Russell syndrome.[7]
Interestingly, patients with Silver–Russell syndrome have variable hypomethylation levels in different body tissues, suggesting a mosaic pattern and a postzygotic epigenetic modification issue. This could explain the body asymmetry frequently seen.[9]
For many years the diagnosis of Silver–Russell syndrome was clinical. However, this led to overlaps with syndromes with similar clinical features such as Temple syndrome and 12q14 microdeletion syndrome.[11] In 2017, an international consensus was published – detailing the steps clinicians should take to diagnose Silver–Russell syndrome.[12] It is now recommended to test for 11p15 loss of methylation and mUPD7 first. If they are negative, then testing for mUPD16, mUPD20 should take place. Testing for 14q32 should also be considered, to rule out Temple syndrome as a differential diagnosis. If these tests come back inconclusive, then a clinical diagnosis should be made.[12]
It is recommended that the Netchine-Harbison clinical scoring system (NH-CSS) is used to group the clinical features together in a point based score.[12]
Treatment
The caloric intake of children with Silver–Russell syndrome must be carefully controlled in order to provide the best opportunity for growth.[2] If the child is unable to tolerate oral feeding, then enteral feeding may be used, such as the percutaneous endoscopic gastrostomy.
In children with limb-length differences or scoliosis, physiotherapy can alleviate the problems caused by these symptoms. In more severe cases, surgery to lengthen limbs may be required. To prevent aggravating posture difficulties children with leg length differences may require a raise in their shoe.[citation needed]
Growth Hormone Therapy is often prescribed as part of the treatment of Silver–Russell syndrome.
The hormones are given by injection typically daily from the age of 2 years old through teenage years. This type of treatment may start to show no effect after or soon before puberty ends. Although there are many other alternative treatments, none seem to work as well as Growth Hormone Therapy.
It may be effective even when the patient does not have a growth hormone deficiency.
Growth hormone therapy has been shown to increase the rate of growth in patients[13] and consequently prompts 'catch up' growth.
This may enable the child to begin their education at a normal height, improving their self-esteem and interaction with other children.
Several studies have shown that growth hormone therapy significantly improves childhood growth and final adult height.[14]
There are some theories suggesting that the therapy also assists with muscular development and managing hypoglycemia.
^Wollmann, H. A.; Kirchner, T; Enders, H; Preece, M. A.; Ranke, M. B. (1995). "Growth and symptoms in Silver-Russell syndrome: Review on the basis of 386 patients". European Journal of Pediatrics. 154 (12): 958–68. doi:10.1007/bf01958638. PMID8801103. S2CID21595433.
^Rakover, Y.; Dietsch, S.; Ambler, G. R.; Chock, C.; Thomsett, M.; Cowell, C. T. (1996). "Growth hormone therapy in Silver Russell Syndrome: 5 years experience of the Australian and New Zealand Growth database (OZGROW)". European Journal of Pediatrics. 155 (10): 851–7. doi:10.1007/BF02282833. PMID8891553. S2CID11550940.
^Silver-Russell Syndrome (2.0 ed.). United Kingdom: Child Growth Foundation. March 2021. p. 19. Retrieved 9 April 2022.
^Silver, H. K.; Kiyasu, W; George, J; Deamer, W. C. (1953). "Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins". Pediatrics. 12 (4): 368–76. doi:10.1542/peds.12.4.368. PMID13099907. S2CID22644845.
